| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35658016-35658318 | Common:5; Rare:213; Clinvar:16; Clinvar (benign):10; Clinvar (pathogenic):29 | ||||
| chr9:35732077-35732646 | Common:4; Rare:159 | ||||
| chr9:35748910-35749354 | Common:3; Rare:151 | ||||
| chr9:36136595-36136778 | Common:2; Rare:57 | ||||
| chr9:36400267-36400344 | Common:1; Rare:18 | ||||
| chr9:37001860-37002199 | Common:3; Rare:88 | ||||
| chr9:37002207-37002293 | Common:1; Rare:14 | ||||
| chr9:37002460-37002771 | Common:1; Rare:84 | ||||
| chr9:37003233-37003344 | Rare:17 | ||||
| chr9:37034036-37034402 | Common:1; Rare:112 | ||||
| chr9:37283925-37284115 | Rare:40 | ||||
| chr9:37284224-37284261 | Rare:7 | ||||
| chr9:37422469-37422744 | Common:7; Rare:118 | ||||
| chr9:37800707-37800819 | Rare:32 | ||||
| chr9:68779907-68780059 | Common:2; Rare:52 |